Clinicopathological and Perioperative Outcome of Appendiceal Tumors: Case Review of 31 Patients

Haroutioun H. Boyajian, Vanessa Majeski, A. Flores, D. Sturtz, Fadi Baidoun, Mohammed Dughayli
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引用次数: 3

Abstract

INTRODUCTION Neoplasms of the appendix are quite rare and found in approximately 1% of appendectomy specimens. These neoplasms have been pathologically categorized into various subgroups depending on cell of origin, and surgical treatment varies according to histological subtype and disease stage. PURPOSE The purpose of this case series review was to evaluate the clinicopathological presentation and survival outcome of a sample of patients with appendiceal tumors. METHODS Before data collection, this project design was approved by the authors’ institutional review board. Pathology records at our institution were reviewed for cases of appendiceal tumors from January 2007 to December 2016. A total of 31 patients were identified over this 10-year period. Retrospective data collection included patient demographics, presenting symptoms, tumor size, histologic diagnosis, initial and secondary management, perioperative and postoperative outcome, and survival benefits. RESULTS Thirty one patients with four different appendiceal tumor subtypes were included in the study: Mucinous Cystadenoma, Mucinous Adenocarcinoma, Goblet Cell, and Carcinoid. The sample was comprised of 17 women (54.8%) and 14 men (45.2%) with an overall mean age of 50.1 (SD = 22.3). Subgroups of 13 (42%) patients had Carcinoid tumor, 12 (39%) had Mucinous Cystadenoma, four (13%) had Goblet cell tumor, and two (6%) had Mucinous Adenocarcinoma. The stage at presentation and tumor size also varied by histologic subtype. The most common presenting symptom was abdominal pain (64.5%), followed by a radiological identified mass (12.9%). Overall, 27 (87.1%) patients survived, and four (12.9%) were deceased. CONCLUSIONS The findings from this case series review provides a retrospective analysis of appendiceal tumor characteristics, follow up, and survival. Based on these results, the prognosis and management of patients with these tumors should be based on the histologic subtype and the extent of their disease.
阑尾肿瘤的临床病理和围手术期结果:附31例病例分析
引言阑尾肿瘤非常罕见,大约1%的阑尾切除标本中都有发现。根据来源细胞的不同,这些肿瘤在病理上被分为不同的亚组,手术治疗根据组织学亚型和疾病分期而不同。本病例系列综述的目的是评估阑尾肿瘤患者的临床病理表现和生存结果。方法在数据收集之前,本项目设计得到了作者机构审查委员会的批准。回顾了2007年1月至2016年12月我院阑尾肿瘤病例的病理学记录。在这10年期间,共确认了31名患者。回顾性数据收集包括患者人口统计学、症状、肿瘤大小、组织学诊断、初次和二次治疗、围手术期和术后结果以及生存益处。结果31例阑尾肿瘤患者分为四种不同的亚型:粘液性囊腺瘤、粘液性腺癌、杯状细胞和类癌。样本包括17名女性(54.8%)和14名男性(45.2%),总体平均年龄为50.1(SD=22.3)。亚组13名(42%)患者患有类癌,12名(39%)患者患有粘液性囊腺瘤,4名(13%)患者患有Goblet细胞瘤,2名(6%)患者患有黏液性腺癌。表现阶段和肿瘤大小也因组织学亚型而异。最常见的症状是腹痛(64.5%),其次是放射学检查发现的肿块(12.9%)。总体而言,27名(87.1%)患者存活,4名(129%)患者死亡。结论本病例系列综述的结果提供了阑尾肿瘤特征、随访和生存率的回顾性分析。基于这些结果,这些肿瘤患者的预后和治疗应基于其组织学亚型和疾病程度。
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